WEE1 kinase protects the stability of stalled DNA replication forks by limiting CDK2 activity

Cell Rep. 2022 Jan 18;38(3):110261. doi: 10.1016/j.celrep.2021.110261.

Abstract

Cellular feedback systems ensure genome maintenance during DNA replication. When replication forks stall, newly replicated DNA is protected by pathways that limit excessive DNA nuclease attacks. Here we show that WEE1 activity guards against nascent DNA degradation at stalled forks. Furthermore, we identify WEE1-dependent suppression of cyclin-dependent kinase 2 (CDK2) as a major activity counteracting fork degradation. We establish DNA2 as the nuclease responsible for excessive fork degradation in WEE1-inhibited cells. In addition, WEE1 appears to be unique among CDK activity suppressors in S phase because neither CHK1 nor p21 promote fork protection as WEE1 does. Our results identify a key role of WEE1 in protecting stalled forks, which is separate from its established role in safeguarding DNA replication initiation. Our findings highlight how WEE1 inhibition evokes massive genome challenges during DNA replication, and this knowledge may improve therapeutic strategies to specifically eradicate cancer cells that frequently harbor elevated DNA replication stress.

Keywords: CDK; DNA replication; WEE1; cancer; cell cycle; fork protection; genome integrity; nucleases; replication stress.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Cycle Proteins / metabolism*
  • Cell Line
  • Cyclin-Dependent Kinase 2 / metabolism*
  • DNA Replication / physiology*
  • Genomic Instability / physiology
  • Humans
  • Protein-Tyrosine Kinases / metabolism*

Substances

  • Cell Cycle Proteins
  • Protein-Tyrosine Kinases
  • WEE1 protein, human
  • CDK2 protein, human
  • Cyclin-Dependent Kinase 2